Canonical Allele Identifier: CA385200981

Gene: RDH5

Linked Data

• MyVariant Identifiers: chr12:g.56115641A>C (hg19) ; chr12:g.55721857A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.55721857A>C , CM000674.2:g.55721857A>C	GRCh38
NC_000012.11:g.56115641A>C , CM000674.1:g.56115641A>C	GRCh37
NC_000012.10:g.54401908A>C	NCBI36
NG_008606.1:g.6491A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000257895.10:c.479A>C MANE Select	ENSP00000257895.6:p.Asn160Thr
ENST00000257895.9:c.479A>C	ENSP00000257895.5:p.Asn160Thr
ENST00000257899.3:c.494A>C
ENST00000547072.5:c.188A>C	ENSP00000449927.1:p.Asn63Thr
ENST00000548082.1:c.479A>C	ENSP00000447128.1:p.Asn160Thr
ENST00000548123.1:c.300+363A>C
ENST00000548486.1:n.489A>C
ENST00000550412.5:c.*151A>C	ENSP00000447650.1:n.*151A>C
ENST00000550608.1:n.618A>C
ENST00000551946.5:c.*282A>C	ENSP00000450201.1:n.*282A>C
ENST00000553160.1:n.406-338A>C
ENST00000553187.5:n.489A>C
NM_001199771.1:c.479A>C	NP_001186700.1:p.Asn160Thr
NM_002905.3:c.479A>C	NP_002896.2:p.Asn160Thr
NR_037658.1:n.538A>C
NM_001199771.2:c.479A>C	NP_001186700.1:p.Asn160Thr
NM_002905.5:c.479A>C MANE Select	NP_002896.2:p.Asn160Thr
NM_001199771.3:c.479A>C	NP_001186700.1:p.Asn160Thr